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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4832719copy number variation1nstd200human GRCh37 chr11: 5,112,289-5,177,946 , GRCh38.p12 chr11: 5,091,059-5,156,716 OR52A5, OR52E3P, 3 more genes
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4729070copy number variation1nstd102humanUncertain significance GRCh37 chr11: 4,970,264-5,225,635 , GRCh38.p12 chr11: 4,949,034-5,204,405 OR52A4P, OR52J2P, 16 more genes
    nsv4680228copy number variation1nstd189human GRCh37.p13 chr11: 4,967,265-5,216,022 , GRCh38.p12 chr11: 4,946,035-5,194,792 OR52A1, OR51A1P, 16 more genes
    nsv4675184copy number variation1nstd102humanPathogenic GRCh37 chr11: 5,112,523-5,336,304 , GRCh38.p12 chr11: 5,091,293-5,315,074 OR52A4P, OR52J1P, 16 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4603042copy number variation1nstd183human GRCh37 chr11: 5,087,330-5,126,489 , GRCh38.p12 chr11: 5,066,100-5,105,259 OR52E1, OR52J1P, 2 more genes
    nsv4387795copy number variation1nstd173human GRCh37 chr11: 5,067,391-6,257,231 , GRCh38.p12 chr11: 5,046,161-6,236,001 HBD, OR52N2, 85 more genes
    nsv4381756copy number variation1nstd173human GRCh37 chr11: 4,167,416-5,153,276 , GRCh38.p12 chr11: 4,146,186-5,132,046 C11orf40, OR51H1, 62 more genes
    nsv4350476copy number variation1nstd102humanPathogenic GRCh37 chr11: 193,146-12,643,136 , GRCh38.p12 chr11: 193,146-12,621,589 KRTAP5-3, OR56A7P, 457 more genes
    nsv4345375sequence alteration1nstd166human GRCh37.p13 chr11: 5,037,622-5,455,788 , GRCh38.p12 chr11: 5,016,392-5,434,558 HBB, HBE1, 32 more genes
    nsv4209216copy number variation1nstd166human GRCh37.p13 chr11: 4,954,871-5,233,023 , GRCh38.p12 chr11: 4,933,641-5,211,793 OR52J1P, OR51A4, 18 more genes
    nsv4206940copy number variation1nstd166human GRCh37.p13 chr11: 4,980,843-5,188,454 , GRCh38.p12 chr11: 4,959,613-5,167,224 OR52E2, OR52A5, 12 more genes
    nsv4192783copy number variation1nstd166human GRCh37.p13 chr11: 4,640,331-5,290,171 , GRCh38.p12 chr11: 4,619,101-5,268,941 HBE1, OR52E1, 50 more genes
    nsv3968644copy number variation1nstd168human GRCh38 chr11: 5,084,095-5,129,619 , GRCh37.p13 chr11: 5,105,325-5,150,849 OR52E3P, OR52A4P, 1 more genes
    nsv3919565copy number variation1nstd102humanPathogenic GRCh38 chr11: 61,793-10,727,969 , GRCh37 chr11: 61,793-10,749,516 , NCBI36 chr11: 51,793-10,706,092 OR51A7, OR51F5P, 437 more genes
    nsv3918376copy number variation1nstd102humanPathogenic NCBI36 chr11: 128,203-5,440,733 , GRCh37.p13 chr11: 138,203-5,484,157 , GRCh38.p12 chr11: 138,203-5,462,927 HBG2, OR51T1, 262 more genes
    nsv3913735copy number variation1nstd102humanPathogenic GRCh37 chr11: 196,855-5,343,104 , GRCh38 chr11: 196,855-5,321,874 , NCBI36 chr11: 186,855-5,299,680 CDKN1C, LOC107984301, 246 more genes
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